scholarly journals Is primary meningococcal arthritis in children more frequent than we expect? Two pediatric case reports revealed by molecular test

2018 ◽  
Vol 18 (1) ◽  
Author(s):  
S. Ricci ◽  
A. Montemaggi ◽  
F. Nieddu ◽  
D. Serranti ◽  
G. Indolfi ◽  
...  
2017 ◽  
Vol 19 (3) ◽  
pp. 339-348 ◽  
Author(s):  
Gregory W. Albert ◽  
Murat Gokden

Solitary fibrous tumors of the spine are rare lesions. Their description in the literature is limited to case reports and small case series. While generally benign lesions, they can recur and occasionally occur as malignancies. Here the authors present the case of a 10-year-old boy, the youngest patient and first preadolescent reported thus far, with this condition. In addition, they perform a comprehensive review of all previously published cases of spinal solitary fibrous tumors.


2017 ◽  
Vol 2017 ◽  
pp. 1-5 ◽  
Author(s):  
Ashish Garg ◽  
Elza Pollak-Christian ◽  
Navneetha Unnikrishnan

A three-month-old female infant presented with abdominal distention for 2 months. A large palpable mass in right upper quadrant was noted on physical exam. Abdominal ultrasound revealed a large heterogeneous mass with multiple cystic components. Mass was surgically excised and pathology was consistent with mature adrenal teratoma. Teratoma is a germ cell tumor mainly found in gonadal tissues. Occurrence of adrenal gland teratoma in children is very rare with less than 10 pediatric case reports in English literature. We present a rare case of primary adrenal tumor in an infant and a review of the literature.


2014 ◽  
Vol 4 (1) ◽  
pp. 39-43 ◽  
Author(s):  
J. T. Nguyen ◽  
R. Shahid ◽  
R. Manera
Keyword(s):  

2021 ◽  
Vol 17 (1) ◽  
Author(s):  
Giovanni Conti ◽  
Nicolina Stefania Carucci ◽  
Valentina Comito ◽  
Pietro Impellizzeri ◽  
Carmela Visalli ◽  
...  

Abstract Background Acute abdominal pain in nephrotic syndrome (NS) is a well-known clinical symptom and is mainly related to peritonitis. The presence, although rare, of red umbilicus may guide the diagnosis as a suggestive sign of peritonitis also in the non-neonatal period. Instead, the association between intussusception and NS is quite limited. We reviewed all published cases in the literature, and to our knowledge, this is one of the few pediatric cases of spontaneous resolution of intussusception in the setting of NS. Finally, a review of the causes of abdominal pain during the course of NS was made. Cases presentation We report two pediatric patient cases who complained of acute abdominal pain during a relapse episode of their NS. The first case is a 4-year-old boy with NS (fourth relapse) who presented with acute abdominal pain, ascites, and red umbilicus. Our suspect of primary peritonitis was clinically confirmed because of the subsequent appearance of the classical peritoneal signs. The second case is a 4-year-old boy who developed an ileo-ileal intussusception during the treatment of his first NS relapse, with spontaneous reduction. Conclusions Gastrointestinal disorders are frequently encountered in the course of NS. The appearance of acute abdominal pain in children with NS requires quick management, both clinical and instrumental. A multidisciplinary team approach needs to be encouraged to lead to an accurate diagnosis and a correct treatment.


2020 ◽  
Vol 38 (4) ◽  
pp. 232
Author(s):  
Yu-Hung Wu ◽  
Hsiao-Yu Li ◽  
Hsiu-Chin Chen

PEDIATRICS ◽  
1982 ◽  
Vol 70 (4) ◽  
pp. 596-596
Author(s):  
T. E. C.

Nineteenth century medical literature abounds with strange pediatric case reports; none is more bizarre than the following, published in 1870 in the Boston Medical and Surgical Journal. AN ELECTRICAL INFANT—There is a wonderful account in all the French papers of an outstanding baby just dead, at the age of ten months, at St Urbain, near Lyons. The strongest medical evidence is said to be given that the child was so highly endowed with electricity that all the persons in the same room with him received constant electric shocks. Its end was apparently painless, but accompanied by still more astounding manifestations. At the instant of death luminous effluvia proceeded, it is affirmed by the doctors, from the body of the child, which continued for several minutes after its decease. The case is supposed to be quite unprecedented in the world of science.


2016 ◽  
Vol 36 (6) ◽  
pp. 680-684 ◽  
Author(s):  
Troy A. Markel ◽  
Karen W. West

Erosion of peritoneal dialysis (PD) catheters into the intestine is a rare complication of PD. Herein, we convey the first reports of 2 pediatric patients undergoing PD who were found to have the catheter eroding into their intestines. They were treated minimally with catheter removal and antibiotics. Definitive repair of the intestinal injury was not performed. These are the first pediatric patients reported with PD catheter erosion. Perforating injuries may be self-limiting, and therefore a more minimal approach may be considered in certain patient populations who do not express overt signs of peritonitis or illness.


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